The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
Chromoselective Photocatalysis: Controlled Bond Activation through Light‐Color Regulation of Redox Potentials
Abstract
Catalysts that can be regulated in terms of activity and selectivity by external stimuli may allow the efficient multistep synthesis of complex molecules and pharmaceuticals. Herein, we report the light‐color regulation of the redox potential of a photocatalyst to control the activation of chemical bonds. Light‐color control of the redox power of a photocatalyst introduces a new selectivity parameter to photoredox catalysis: Instead of changing the catalyst or ligand, alteration of the color of the visible‐light irradiation adjusts the selectivity in catalytic transformations. By using this principle, the selective activation of aryl–halide bonds for C−H arylation and the sequential conversion of functional groups with different reduction potentials is possible by simply applying different colors of light for excitation of the photocatalyst.
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Visible light photoredox catalysis: applications in organic synthesis
Narayanam, J. M. R., & Stephenson, C. R. J. (2011) · Chem. Soc. Rev. · doi:10.1039/b913880n · Cited by 4,161
Receptors for Purines and Pyrimidines
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Visible light photocatalysis as a greener approach to photochemical synthesis
Yoon, T. P., Ischay, M. A., & Du, J. (2010) · Nature Chemistry · doi:10.1038/nchem.687 · Cited by 2,657
Subdiffraction‐Resolution Fluorescence Imaging with Conventional Fluorescent Probes
Heilemann, M., van de Linde, S., Schüttpelz, M., Kasper, R., Seefeldt, B., Mukherjee, A., Tinnefeld, P., & Sauer, M. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200802376 · Cited by 1,866
Multicolor Super-Resolution Imaging with Photo-Switchable Fluorescent Probes
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Controlling Site Selectivity in Palladium-Catalyzed C–H Bond Functionalization
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Reduction of aryl halides by consecutive visible light-induced electron transfer processes
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Self-citationDirect stochastic optical reconstruction microscopy with standard fluorescent probes
van de Linde, S., Löschberger, A., Klein, T., Heidbreder, M., Wolter, S., Heilemann, M., & Sauer, M. (2011) · Nature Protocols · doi:10.1038/nprot.2011.336 · Cited by 1,071
Cited by
Visible Light Mediated Photoredox Catalytic Arylation Reactions
Ghosh, I., Marzo, L., Das, A., Shaikh, R., & König, B. (2016) · Accounts of Chemical Research · doi:10.1021/acs.accounts.6b00229 · Cited by 782
Self-citationSpeckmeier, E., Fischer, T. G., & Zeitler, K. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b08933 · Cited by 771
Tay, N. E. S., Lehnherr, D., & Rovis, T. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00384 · Cited by 518
Photoredox Catalytic Organic Transformations using Heterogeneous Carbon Nitrides
Savateev, A., Ghosh, I., König, B., & Antonietti, M. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201802472 · Cited by 477
Self-citationSynthetic Photoelectrochemistry
Barham, J. P., & König, B. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.201913767 · Cited by 448
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Metadata
- Authors
- Ghosh, I., & König, B.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2016-05-20
- Volume
- 55
- Issue
- 27
- Pages
- 7676-7679
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2408631314
- Cited by
- 377
- References
- 24
- FWCI
- 18.86
- Type
- journal article
- Language
- en
- Open access
- closed
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